Analysis of barley chloroplast psbD light-responsive promoter elements in transplastomic tobacco

Plant Molecular Biology - Tập 47 - Trang 353-366 - 2001
Karen E. Thum1, Minkyun Kim1, Daryl T. Morishige1, Christian Eibl2, Hans-Ulrich Koop2, John E. Mullet1
1Department of Biochemistry and Biophysics, Texas A&M University, College Station, USA
2Botanical Institute, Ludwig-Maximilians-Universität, Munich, Germany

Tóm tắt

The plastid gene psbD encodes D2, a photosystem II reaction center chlorophyll-binding protein. psbD is transcribed from a conserved chloroplast promoter that is activated by blue, white, or UV-A light. In this study, various forms of the barley (Hordeum vulgare L.) chloroplast psbD-LRP were fused to the uidA reporter gene and introduced into the tobacco (Nicotiana tabacum L.) plastid genome through homologous recombination. Primer extension analysis of transcripts from the psbD-LRP-uidA construct showed that the barley psbD-LRP was activated in tobacco by blue or white light. Transcription from this construct was also regulated by circadian cycling indicating that the barley psbD-LRP could respond to light modulated regulatory pathways in tobacco. Mutation of the psbD-LRP prokaryotic −10 promoter element reduced transcription to very low levels in all light regimes. In contrast, mutation of a prokaryotic −35 promoter element had no effect on transcription from the psbD-LRP. Deletion or mutation of an upstream activating element, the AAG-box (−36 to −64), also reduced transcription from the construct to very low levels. In contrast, deletion of the upstream PGT-box (−71 to −100) did not alter promoter activation by blue light, or responsiveness to circadian cycling. These in vivo studies confirm the importance of the psbD-LRP −10 promoter element and AAG-box in light regulation and demonstrate that these elements are sufficient to mediate circadian cycling of the barley psbD promoter.

Tài liệu tham khảo

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